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Typical nemaline myopathy

MONDO:0015737

Typical nemaline myopathy is a moderate neonatal form of nemaline myopathy (NM) characterized by facial and skeletal muscle weakness and mild respiratory involvement.

Also known as: typical congenital nemaline myopathy

37 clinical trials for this condition and its sub-types.

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Sub-types

Congenital myopathy 23 (0) Congenital myopathy 2a, typical, autosomal dominant (0) Nemaline myopathy 10 (0) Nemaline myopathy 2 (0) Nemaline myopathy 7 (0) Nemaline myopathy 9 (0)

Broader categories

Disease (618) Nervous system disorder (217) Musculoskeletal system disorder (196) Hereditary disease (172) Muscle tissue disorder (53) Human disease (14) Nemaline myopathy (13) Myopathy (11) Congenital myopathy (8) Skeletal muscle disorder (8)

Trials to join now! 18 Not yet recruiting 7 Not yet finished but already full! 4 Completed 7 Terminated 1

Scientists gather leftover surgical tissue to unlock secrets of bone disease

Knowledge-focused Terminated

This study collected bone, cartilage, skin, and fat tissue from 50 patients undergoing surgery at Children's National Medical Center. The goal was to grow cells from these tissues in the lab and analyze them to better understand bone and connective tissue diseases. The study was …

Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

Last updated Jun 27, 2026 07:52 UTC